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CORDIS OPTA 5(TM) PTA BALLOON CATHETER, MODIFICATION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940868
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/1994
Days to Decision
140 days
Submission Type
Summary

CORDIS OPTA 5(TM) PTA BALLOON CATHETER, MODIFICATION

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940868
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/1994
Days to Decision
140 days
Submission Type
Summary